17513075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78098668-G-A

17513075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78098668-G-T

17513135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78098725-G-A

17513135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78098725-G-C

17513135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78098725-G-T

17513168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78098758-A-G

17513308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78098887-G-A

17513308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78098887-G-T

17513369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78098957-G-C

17513421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099021-A-G

17513612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099200-G-A

http://identifiers.org/hco/21/GRCh38#17513742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78099318-C-A

17514219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099754-A-G

17514221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099756-G-T

17514372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099912-T-C

http://identifiers.org/hco/21/GRCh38#17514428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78099975-C-A

17514540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78100061-G-T

17514628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78100103-G-T

17516027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78100655-A-G

17516040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78100667-A-G

http://identifiers.org/hco/21/GRCh38#17516186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78101106-C-A

17519667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78102784-C-T

17520535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78103581-C-G

17522469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78105254-G-A

17522470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78105255-A-G

17522772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78105986-G-T

17522793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78106007-A-G

17523211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78106384-A-G

17523289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78106465-T-A

17523356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78106514-A-G

17523453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78106607-C-G

17523608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78106766-G-A

17525053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78108940-G-A

17525072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78108959-A-G

17525135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109027-A-G

17525423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109252-C-T

17525470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109305-C-T

17525491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109329-T-C

17525562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109405-C-T

17525666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109497-T-C

17526301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110304-T-G

17526533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110536-A-G

17526533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110536-A-T

17526855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110759-T-C

17526902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110805-C-T

17527001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110905-C-T

17527033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110942-C-T

17527064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110973-T-C

17527174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78111037-G-A

17527174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78111037-G-T

17527176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78111039-A-G

17527368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78111147-G-A

17533040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78113522-A-G

17533503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78114167-A-G

http://identifiers.org/hco/21/GRCh38#17533529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78114191-C-A

17533860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78114609-A-G

http://identifiers.org/hco/21/GRCh38#17534030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78114756-C-A

17534147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78114836-A-G

17534199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78114892-C-T

17539443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116290-A-G

17539720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116581-T-A

17539880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116685-A-G

17540062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116815-G-A

17540067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116820-T-C

17540086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116838-G-C

17540102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116853-C-T

17540104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116855-G-A

17540160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116902-C-G

17540160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116902-C-T

17540226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116924-A-G

17540306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116989-C-T

17540307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116990-G-A

17540309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116992-C-T

17540315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78116998-C-G

17540490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78117153-G-A

17540522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78117174-A-T

17540586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78117216-G-A

17540596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78117226-A-G

17541858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118123-G-A

17541947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118187-T-C

17542030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118250-T-A

http://identifiers.org/hco/21/GRCh38#17542117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78118359-C-A

http://identifiers.org/hco/21/GRCh38#17542157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78118395-A-C

17542180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118421-T-C

17542377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118626-A-T

17542585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78118823-C-T

17542599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118837-A-G

17542693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118930-C-T

17542694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118931-G-A

17542694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118931-G-T

17542696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118933-A-G

17542762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78118985-C-G

http://identifiers.org/hco/21/GRCh38#17542770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#78118993-C-A

17542799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78119022-G-A

17542870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119079-C-G

17542870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119079-C-T

17542915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119125-T-C

17543012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119228-T-A

17543012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119228-T-C

17543030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119246-A-G

17543030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119246-A-T

17543043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119259-G-A

17543043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78119259-G-T

17544370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120042-A-G

17544478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120149-G-A

17544579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120287-G-A

17544796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120478-A-G

17544805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120487-G-A

17545033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120637-G-C

17545050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120655-A-T

17545176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120782-C-T

17545223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78120830-A-G

17546880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78121935-T-A

http://identifiers.org/hco/21/GRCh38#17547238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78122259-C-A

17547285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78122286-G-A

http://identifiers.org/hco/21/GRCh38#17547327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78122323-C-A

17547338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78122334-A-G

17547340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78122336-G-A

17547454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78122421-G-A

http://identifiers.org/hco/21/GRCh38#17548493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78123543-C-A

17548493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123543-C-G

17548494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123544-T-A

17548616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123639-C-G

17548616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123639-C-T

17548868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123832-C-G

17548872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123836-G-T

17548934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123904-G-T

17548938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123908-A-T

17548946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123916-G-A

17548948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123918-A-G

17548948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78123918-A-T

http://identifiers.org/hco/21/GRCh38#17548982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78123955-C-A

17549128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124181-G-A

17549333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124622-A-T

17549347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124636-T-C

17549414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124697-T-A

17549473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124742-A-G

17549708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124971-C-T

17549749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78124988-C-T

17549957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78125129-A-G

17551841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78125934-T-A

17551841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78125934-T-C

17552114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78126215-A-G

17553303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78127717-T-A

17553359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78127774-G-C

http://identifiers.org/hco/21/GRCh38#17553474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78127874-A-C

17557302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78128642-C-T

17557494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78128813-G-A

17557519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78128831-A-G

17557589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78128895-A-G

17558418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78129677-G-A

17558575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78129841-G-T

17558900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130142-G-T

17558953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130224-T-G

http://identifiers.org/hco/21/GRCh38#17559134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78130408-A-C

http://identifiers.org/hco/21/GRCh38#17559540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78130516-A-C

17559540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130516-A-G

17559633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130605-T-C

17560472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130843-G-T

17560551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130909-T-G

17560555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130913-T-A

17560570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130926-T-G

17560572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130928-G-T

17560624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130975-A-G

17560631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78130983-T-C

17560652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131004-A-G

17560655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131007-A-G

17560733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78131088-T-C

17560805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78131160-G-A

17560903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131258-T-G

http://identifiers.org/hco/21/GRCh38#17560912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78131267-C-A

17561107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131442-C-T

17561125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131448-T-C

17561222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131534-T-A

17561222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131534-T-C

17561222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131534-T-G

http://identifiers.org/hco/21/GRCh38#17561268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78131634-A-C

17561268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131634-A-G

17561270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131636-A-G

17561294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131660-G-A

17561311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131676-T-C

17561324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131689-T-C

17561360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78131732-T-C

17561525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131894-T-C

17561572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131940-T-C

17561573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131941-T-C

17561573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131941-T-G

17561594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131952-T-G

http://identifiers.org/hco/21/GRCh38#17561627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78131985-C-A

17561627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78131985-C-T

17561857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78132256-A-T

17561908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78132306-G-A

17562002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78132397-G-A

17565104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78132840-A-G

17565383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78133029-T-A

17565397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78133044-C-G

17565407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78133055-A-G

17565518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78133166-C-G

17565644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78133292-G-A

http://identifiers.org/hco/21/GRCh38#17565662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78133310-A-C

17565687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78133335-G-C

17565793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133443-T-A

http://identifiers.org/hco/21/GRCh38#17565794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78133444-C-A

17565840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133581-T-A

17565840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133581-T-C

17565840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133581-T-G

http://identifiers.org/hco/21/GRCh38#17566070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78133808-C-A

17566070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133808-C-T

17566135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133872-T-C

17566135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133872-T-G

17566162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133897-A-T

17566217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78133948-A-G

17566312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134173-A-G

17566408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134268-T-G

17566416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134274-A-G

17566420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134278-A-G

17566438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134296-G-A

17566438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134296-G-T

17566495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134338-G-T

17566546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134411-C-T

17566603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134522-T-C

17566625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134541-T-A

17566665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134561-T-G

17566672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134568-T-A

17566735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134621-G-T

17566867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134749-A-G

17567024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134867-A-G

17567024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78134867-A-T

17567317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78135165-T-G

http://identifiers.org/hco/21/GRCh38#17567353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78135204-A-C

17567353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78135204-A-G

17567526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78135375-C-G

http://identifiers.org/hco/21/GRCh38#17567555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78135407-C-A

http://identifiers.org/hco/21/GRCh38#17567743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78135571-C-A

http://identifiers.org/hco/21/GRCh38#17568462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78136070-C-A

17568462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136070-C-G

17568474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136082-T-C

17568499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136105-T-C

17568758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136208-A-G

17568777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136227-G-A

17568777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136227-G-C

17568777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136227-G-T

http://identifiers.org/hco/21/GRCh38#17568798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78136244-A-C

http://identifiers.org/hco/21/GRCh38#17568893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78136334-C-A

17568958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136452-A-G

17568978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136538-G-T

17569020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136613-C-T

17569137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136711-C-T

17569190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136780-G-A

17569190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136780-G-C

17569190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136780-G-T

17569263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78136852-G-A

17569569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78137141-T-C

17569630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78137186-G-A

17569671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78137232-C-T

http://identifiers.org/hco/21/GRCh38#17569697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78137251-A-C

17569701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78137255-A-G

17569985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78137526-C-T

17570191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78137731-G-A

17570191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78137731-G-T

http://identifiers.org/hco/21/GRCh38#17570211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78137748-C-A

17570211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78137748-C-G

http://identifiers.org/hco/21/GRCh38#17570214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78137751-C-A

http://identifiers.org/hco/21/GRCh38#17570346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78137886-A-C

17570414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78137973-G-A

17570414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78137973-G-C

17570473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138040-G-T

17570574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138117-A-G

17570635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138178-C-T

17570640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138183-C-T

17570752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138248-G-A

17570870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138361-T-C

17571348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78138788-T-C

17571673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78139115-A-G

17582599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78140890-C-T

17582810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78141099-T-C

http://identifiers.org/hco/21/GRCh38#17582866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78141146-C-A

17583381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78141565-T-C

17583509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78141685-C-T

17583682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78141849-A-G

17586000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78143708-G-A

17589640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145329-C-G

17589646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145335-C-T

17589651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145341-G-T

17589784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145455-T-C

17589903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145629-A-G

17589929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145655-C-T

17590029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145780-A-T

17590112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145820-C-T

17590140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145846-A-G

http://identifiers.org/hco/21/GRCh38#17590208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78145905-A-C

17590209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145906-G-A

17590326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78145979-T-G

17590617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146206-G-C

17590713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146304-A-G

http://identifiers.org/hco/21/GRCh38#17590742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78146333-A-C

17590882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146562-A-T

17591048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146775-G-A

17591162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146877-G-A

17591230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78146922-T-G

17591753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78154419-C-T

17591936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78154556-G-A

17592769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78155623-A-T

17592898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78155796-A-T

http://identifiers.org/hco/21/GRCh38#17592955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78155881-A-C

17593086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78156041-T-C

17593274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156226-A-G

17593287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156239-G-A

17593287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156239-G-T

17593306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156417-T-G

17593369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156479-T-C

17593397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156508-A-T

17593457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156579-A-G

http://identifiers.org/hco/21/GRCh38#17593731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#78156829-C-A

17593731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78156829-C-T

17594679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78157758-T-C